U.S. flag

An official website of the United States government

nsv7043910

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:104,253

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 440 SVs from 56 studies. See in: genome view    
    Submitted genomic173,983,915-174,088,167Question Mark
    Overlapping variant regions from other studies: 443 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):173,953,053-174,057,305Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043910Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1173,983,915174,088,167
    nsv7043910RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1173,953,053174,057,305

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743966inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743966Submitted genomicNC_000001.11:g.173
    983915_174088167in
    v
    GRCh38 (hg38)NC_000001.11Chr1173,983,915174,088,167
    nssv18743966RemappedPerfectNC_000001.10:g.173
    953053_174057305in
    v
    GRCh37.p13First PassNC_000001.10Chr1173,953,053174,057,305

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv187439664e-061276268
    Support Center